RS138396764 TRPV4
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Associated Conditions
Charcot-Marie-Tooth disease axonal type 2C
Spondylometaphyseal dysplasia
Kozlowski type
Brachyrachia (short spine dysplasia)
Neuronopathy
distal hereditary motor
autosomal dominant 8
Metatropic dysplasia
Scapuloperoneal spinal muscular atrophy
Connective tissue disorder
Inborn genetic diseases
Charcot-Marie-Tooth disease axonal type 2C
Spondylometaphyseal dysplasia
Kozlowski type
Brachyrachia (short spine dysplasia)
Other Variants in TRPV4